ID: ALA589330

Max Phase: Preclinical

Molecular Formula: C21H24ClN3O3

Molecular Weight: 401.89

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCC(C)[C@H](NC(=O)c1ccc(OC)cc1)C(=O)N/N=C/c1ccc(Cl)cc1

Standard InChI:  InChI=1S/C21H24ClN3O3/c1-4-14(2)19(24-20(26)16-7-11-18(28-3)12-8-16)21(27)25-23-13-15-5-9-17(22)10-6-15/h5-14,19H,4H2,1-3H3,(H,24,26)(H,25,27)/b23-13+/t14?,19-/m0/s1

Standard InChI Key:  ACAMZSYTMVQLCS-HJKLDDSWSA-N

Associated Targets(non-human)

Simian immunodeficiency virus 338 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Structural capsid protein 291 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 401.89Molecular Weight (Monoisotopic): 401.1506AlogP: 3.64#Rotatable Bonds: 8
Polar Surface Area: 79.79Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.66CX Basic pKa: 1.40CX LogP: 4.21CX LogD: 4.21
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.52Np Likeness Score: -1.24

References

1. Jin Y, Tan Z, He M, Tian B, Tang S, Hewlett I, Yang M..  (2010)  SAR and molecular mechanism study of novel acylhydrazone compounds targeting HIV-1 CA.,  18  (6): [PMID:20188575] [10.1016/j.bmc.2010.02.003]

Source